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TiME 之问:微环境相互作用如何塑造 CLL 与 Richter 转化的免疫治疗应答

英文原题:A question of TiME: how microenvironmental interactions shape response to immunotherapy in CLL and Richter Transformation.

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A question of TiME: how microenvironmental interactions shape response to immunotherapy in CLL and Richter Transformation.

PubMed 2025/05/29(内容时间) Front Immunol Q1 · IF 7(JCR 2025)

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中文摘要

免疫治疗已经彻底改变了许多癌症的治疗格局,包括一些B细胞淋巴瘤。免疫检查点阻断、CAR-T 细胞和双特异性抗体在治疗Richter转化(RT)方面显示出前景,但在慢性淋巴细胞白血病(CLL)中表现出活性降低。这些观察结果表明,除了CLL细胞与转化后的RT细胞之间的内在差异外,这两种实体在肿瘤免疫微环境(TiME)组成和肿瘤-免疫细胞相互作用方面也存在显著差异,而这些差异仍有待充分表征。在本视角中,我们重点介绍近期利用患者来源组织和新型小鼠模型描述CLL和RT中TiME的研究。随后,我们简要概述当前在CLL和RT中采用免疫治疗的临床试验,并对该领域当前面临的挑战和未来研究方向提供展望。

展开英文摘要原文

Immunotherapy has revolutionized the treatment landscape for many cancers, including some B- cell lymphomas. Immune checkpoint blockade, CAR-T cells and bispecific antibodies have shown promise for the treatment of Richter Transformation (RT) but have displayed reduced activity in chronic lymphocytic leukemia (CLL).

These observations suggest that, besides the intrinsic differences between CLL cells and transformed RT cells, there are also marked differences in tumor immune microenvironmental (TiME) composition and tumor-immune cell interactions between these two entities, which remain to be fully characterized. In this perspective, we highlight recent studies describing the TiME in CLL and RT, utilizing both patient-derived tissues and novel mouse models.

We then provide a brief overview of current clinical trials employing immunotherapy in CLL and RT and offer a perspective on current challenges and future research efforts in the field.

论文信息

作者
Vom Stein AF、Nguyen PH、Ten Hacken E
第一作者单位
Faculty of Medicine and University Hospital Cologne, Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, University of Cologne, Cologne, Germany.Germany
通讯作者单位
Department of Medicine, Division of Hematology and Oncology, Weill Cornell Medicine, New York City, NY, United States.United States
文献类型
综述
期刊
Frontiers in immunology2025
原文标识
PubMed 40510357 · DOI 10.3389/fimmu.2025.1592574